Ethyl Trifluoroacetate TCI T0432

Chemical Identity

CAS No.: 383-63-1
PubChem: CID 9794·SID 87576384
Formula: C4H5F3O2
Molecular weight: 142.08 g/mol
Purity: >99.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 2,2,2-trifluoroacetate
SMILES: CCOC(=O)C(F)(F)F
InChIKey: STSCVKRWJPWALQ-UHFFFAOYSA-N

Rp 795.900,00

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Ethyl Trifluoroacetate is a chemical compound widely used as a building block in various chemical reactions, particularly in the synthesis of organic compounds containing fluorine. Its unique molecular structure, featuring three fluorine atoms bonded to a carbonate group, makes it a valuable reagent in organic chemistry. In the laboratory, it serves as a key reactant or auxiliary material in the formation of complex compounds such as esters and fluorinated molecules. Due to its reactivity, it is a preferred choice for organic synthesis and molecular research.

This compound is known for its chemical stability under specific conditions, although it is highly reactive towards water and excessive heat. It has a high boiling point and good solubility in organic solvents like ethyl acetate and chloroform. These properties make it suitable for reactions requiring both reactivity and stability. Additionally, its distinct aroma allows for easy detection during laboratory procedures.

In Indonesian laboratories, Ethyl Trifluoroacetate is commonly used by chemists, pharmacists, and material scientists. Its versatility and effectiveness in various synthetic processes make it an essential component in both academic and industrial research settings. Its applications span across multiple disciplines, supporting the development of new materials and pharmaceuticals.

TCI brochures (PDF)

Fluorous Chemistry 2025-01-21 · p. 7
Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 54

Related TCI products

Organic synthesis where fluorinated compounds are required due to its reactivity and fluorine content.
Esterification reactions as a versatile reagent for forming ester functional groups.
Fluorination processes in the development of new pharmaceuticals and materials.
Research in material science for creating fluorinated polymers and coatings.
Analytical chemistry for use in chromatographic and spectroscopic studies due to its distinct chemical properties.

Brand	TCI
CAS number	383-63-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from heat and moisture

Ethyl Trifluoroacetate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its stability. Due to its reactivity with water, it should not be stored near aqueous solutions or in humid conditions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize inhalation risks. Always follow standard safety protocols when working with reactive chemicals to maintain a safe laboratory environment.

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